Amoxicillin Capsule
Product Images NDC 0781-2613

9 FDA label images from Sandoz Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Amoxicillin (NDC 0781-2613). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Amoxicillin 01

Amoxicillin 01
Chemical structure of Amoxicillin monohydrate, showing its molecular components including hydroxyl, amine, amide, carboxyl groups, and a sulfur atom within a beta-lactam ring, along with the 3 molecules of water of hydration.*
FDA Label Image

Amoxicillin 02

Amoxicillin 02
Amoxicillin Capsules, USP 250 mg oral dosage form in a pharmacy bulk package containing 100 capsules. The label includes dosing instructions, storage conditions at 20° to 25°C, and notes that the package is not child resistant. Manufactured by Sandoz Inc for distribution.*
FDA Label Image

Amoxicillin 03

Amoxicillin 03
Amoxicillin Capsules USP 500 mg oral capsules label from Sandoz Inc, showing a pharmacy bulk package containing 100 capsules. The label includes storage and handling instructions, emphasizing the product is not child resistant and requires a tight, light-resistant container.*
FDA Label Image

Amoxicillin 04

Amoxicillin 04
Amoxicillin Tablets, USP 500 mg film-coated tablets packaging label. The label states the package contains 100 tablets, is prescription-only, and is manufactured by Sandoz Inc. It notes that this is a pharmacy bulk package that is not child-resistant and includes storage instructions and dosage guidelines.*
FDA Label Image

Amoxicillin 05

Amoxicillin 05
Label for Amoxicillin Tablets, USP 875 mg oral capsules from Sandoz Inc. The label shows 100 tablets per package and specifies the product is prescription only. It includes storage instructions, notes the package is not child resistant, and provides manufacturer details as Sandoz GmbH for Sandoz Inc., Princeton, NJ.*
FDA Label Image

Amoxicillin 06

Amoxicillin 06
Amoxicillin for Oral Suspension USP 125 mg/5 mL oral suspension. The label states it is Rx only and describes that each 5 mL contains amoxicillin trihydrate equivalent to 125 mg amoxicillin. The total volume when reconstituted is 80 mL. The product is labeled by Sandoz Inc and includes preparation and dosage instructions, a barcode, and storage information.*
FDA Label Image

Amoxicillin 07

Amoxicillin 07
Label for Amoxicillin for Oral Suspension, USP, 200 mg/5 mL, a human prescription drug by Sandoz Inc. This 50 mL bottle contains powder for oral suspension that delivers 200 mg amoxicillin per 5 mL when reconstituted. The label includes directions for mixing, dosage instructions, storage, and manufacturing details.*
FDA Label Image

Amoxicillin 08

Amoxicillin 08
Label for Amoxicillin for Oral Suspension, USP with a strength of 250 mg/5 mL. The label indicates the product is an oral suspension to be reconstituted to 80 mL total volume and is labeled Rx Only. It shows the labeler as Sandoz Inc. Additional details include dosing information and storage instructions, with a statement of contents and NDC 0781-6041-58 visible on the label.*
FDA Label Image

Amoxicillin 09

Amoxicillin 09
Amoxicillin for Oral Suspension, USP 400 mg/5 mL powder for reconstitution label by Sandoz Inc. Each 5 mL of reconstituted suspension contains amoxicillin trihydrate equivalent to 400 mg amoxicillin. The bottle contains 50 mL when reconstituted. Directions for mixing and storage instructions are provided along with the NDC 0781-6157-52.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.